1-tert-Butyl 3-methyl piperazine-1,3-dic, arboxylate, 10 g

Catalog nr. 2E7K.3
Carl Roth

Volume: 10 g
Value Packs: 1 piece
Price:
Sale price€274,15
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Description

1-tert-Butyl 3-methyl piperazine-1,3-dicarboxylate is a differentially protected piperazine derivative for laboratory and research applications. The compound is identified by CAS number 129799-08-2 and the empirical formula C₁₁H₂₀N₂O₄, with a molar mass of 244,29 g/mol. The dual carboxylate substitution pattern—tert-butyl at N-1 and methyl at the 3-position—provides orthogonal handles that are frequently exploited in heterocyclic and medicinal-chemistry synthesis. It is supplied in a 100 g pack, suitable for repeated small-scale reactions as well as intermediate campaign work. Available from manufacturer Carl ROTH within a broader portfolio of research chemicals and biochemicals, the material supports route scouting, building-block elaboration, and preparation of more complex piperazine scaffolds. Clear CAS, formula, and molar-mass data simplify weighing, documentation, and transfer of methods between sites. The 100 g unit quantity offers economical access for groups that consume protected piperazines regularly while remaining manageable for standard laboratory storage and handling. This diester is positioned as a practical intermediate wherever selective deprotection or further functionalisation of the piperazine core is required.

This article is part of Click chemistry, bioconjugation & synthesis reagents, in Organic chemicals & synthesis reagents.

Key features

  • Pack sizes: 10 g, 25 g, 50 g
  • Molar mass: 244,29 g/mol
  • Technical Information Sheet: PDF
  • Safety Data Sheet: PDF

Compliance & Safety Information

GHS07 Warning

Hazard Statements (H-Phrases)

H315 Causes skin irritation
H319 Causes serious eye irritation
H335 May cause respiratory irritation

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Questions about 1-tert-Butyl 3-methyl piperazine-1,3-dic, arboxylate, 10 g

What is this article?

1-tert-Butyl 3-methyl piperazine-1,3-dic, arboxylate, 10 g is the article on this page. Luminix Health distributes Carl Roth for laboratory use. It sits in Click chemistry, bioconjugation & synthesis reagents, inside Organic chemicals & synthesis reagents, in Lab chemicals.

Click and bioconjugation reagents join two molecules under mild conditions, often an azide to an alkyne, or an NHS ester to an amine. The linker length and the reactive group are the specification. They are small bottles of a reactive compound, and moisture often ruins them.

An organic chemical is built on carbon. In this category it is a building block or a reagent for making another molecule: a starting material, a coupling agent, a polymer, a PEG. Purity is a specification of which impurities remain. The structure, the CAS number and the grade decide whether two bottles are the same substance. Structures and properties are on PubChem. Nomenclature is IUPAC. Classification follows ECHA and the CLP Regulation.

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